## Abstract Experiments on the effects of 0.025β0.40 Β΅g of dibutyltin dichloride (DBTCl) per kilogram body weight (kg bw), on sperm density, viability and morphology in mature mice were conducted by daily intraperitoneal injection for 7 days at 22β Β±β 2βΒ°C and 12β h lightβdark cycle conditions. The re
Effect of neonatal exposure to diethylstilbestrol and tamoxifen on pelvis and femur in male mice
β Scribed by Fukazawa, Yugo ;Nobata, Sigenori ;Katoh, Miho ;Tanaka, Masami ;Kobayashi, Sinji ;Ohta, Yasuhiko ;Hayashi, Yokichi ;Iguchi, Taisen
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 894 KB
- Volume
- 244
- Category
- Article
- ISSN
- 0003-276X
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β¦ Synopsis
Background: Permanent abnormalities have been reported in reproductive and non-reproductive organs of mice and humans exposed perinatally to a synthetic estrogen, diethylstilbestrol (DES). Recent studies demonstrated that sex hormones affected the shape of the innominate bone in mice. Therefore, we analyzed the long-term effects of neonatal exposure of DES and tamoxifen, an anti-estrogen, in mouse bones.
Methods: Changes in the pelvis and femur were examined in 1-to 15month-old C57BL/Tw male mice given 5 daily injections of 3 pg DES or of 100 pg tamoxifen beginning on the day of birth by measuring contents of calcium (Ca) and phosphorus (P), and the numbers of osteoblasts and os- teoclasts.
Results: The ash weight of pelvis and femur in neonatally DES-and tamoxifen-treated mice was lower than that in the controls at %15 months of age. Contents of Ca and P of pelvis and femur in neonatally tamoxifentreated mice were lower than in the controls and neonatally DES-treated mice. In neonatally DES-treated mice at 6-12 months, Ca and P contents in the pelvis were lower than in controls, but not different in the femur. The number of osteoblasts per unit length of endocortical surface of the femur in 2-and 3-month-old DES-and tamoxifen-treated mice was lower than that in the controls. The osteoclast number in the femur in DES-treated mice at 2 to 12 months was not different from that in the controls; however, in tamoxifen-treated mice, the number was higher than in the controls. An epiphyseal line was clearly detected in the femur of 12-and 15-month-old DES-and tamoxifen-treated male mice, whereas the line in the controls disappeared after 12 months.
Conclusions: The present results indicate that in male mice, neonatal exposure to DES and tamoxifen induced permanent changes in the pelvis and the femur, and that tamoxifen had a greater effect on bone tissue than did DES.
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